chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	31463347	31463348	C	-	13	GENIC	homozygous	51391625
10	31463500	31463508	AACAACAA	--------	6	GENIC	homozygous	53331466
10	31465463	31465464	T	G	19	GENIC	homozygous	51391627
10	31465772	31465773	T	TG	9	GENIC	homozygous	53137147
10	31467199	31467200	G	GT	25	GENIC	homozygous	53137149
10	31467453	31467454	T	C	36	GENIC	homozygous	51391631
10	31467927	31467928	T	-	11	GENIC	homozygous	51835473
10	31468732	31468733	T	A	20	GENIC	homozygous	51391632
10	31470005	31470006	T	TG	4	GENIC	homozygous	51391633
10	31470167	31470168	A	-	19	GENIC	homozygous	51391634
10	31470181	31470182	T	-	19	GENIC	homozygous	51391635
10	31470418	31470419	T	TCCC	23	GENIC	homozygous	51391636
10	31471097	31471098	T	A	26	GENIC	homozygous	51391638
10	31472945	31472946	T	A	22	GENIC	homozygous	51391642
10	31473340	31473341	T	G	22	GENIC	homozygous	51391645
10	31473627	31473628	G	GCA	8	GENIC	possibly homozygous	53137151
10	31473672	31473673	G	GAC	16	GENIC	possibly homozygous	53137153
10	31474193	31474194	A	-	19	GENIC	possibly homozygous	52185633
10	31475327	31475328	C	T	21	GENIC	homozygous	53137155
10	31473075	31473115	TTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC	----------------------------------------	12	GENIC	homozygous	52315964